Anesthetic Challenges in a Patient With TANGO2 Gene Deletion, DiGeorge Syndrome, and Tetralogy of Fallot: A Case Report

IF 1.1 Q3 ANESTHESIOLOGY
Ivana Wrobleski, Nischal K. Gautam, Richard M. Hubbard
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引用次数: 2

Abstract

Mutations of the transport and Golgi organization 2 (TANGO2) genes are linked with both long-term neurological decline and acute metabolic crises during stress, leading to significant anesthetic risk. Crises are marked by rhabdomyolysis, lactic acidosis, seizures, cardiac dysfunction, and dysrhythmias. Much is unknown about optimal management of this condition, especially in the acute and critical care settings. The following report describes the anesthetic challenges of a patient with simultaneous TANGO2 gene deletion, DiGeorge Syndrome, and Tetralogy of Fallot, who presented for an interventional cardiac procedure with the goal of metabolic crisis-avoidance and facilitation of safe but expeditious recovery and discharge home.
TANGO2基因缺失、DiGeorge综合征和法洛四联症患者的麻醉挑战:一例报告
运输和高尔基体组织2(TANGO2)基因的突变与长期神经系统衰退和应激期间的急性代谢危机有关,导致显著的麻醉风险。危象的特点是横纹肌溶解症、乳酸酸中毒、癫痫发作、心脏功能障碍和心律失常。这种情况的最佳管理还有很多未知之处,尤其是在急性和危重症护理环境中。以下报告描述了一名同时患有TANGO2基因缺失、DiGeorge综合征和法洛四联症的患者的麻醉挑战,该患者提出了一项介入性心脏手术,目的是避免代谢危机,促进安全但快速的康复和出院回家。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
3.60
自引率
14.30%
发文量
31
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